grant

All holographic two-photon electrophysiology

Organization UNIVERSITY OF CALIFORNIA BERKELEYLocation BERKELEY, UNITED STATESPosted 1 Jun 2023Deadline 31 May 2026
NIHUS FederalResearch GrantFY20232-photon3-D3-Dimensional3DAccelerationAction PotentialsAddressAlgorithmsAnimalsArtifactsBRAIN initiativeBenchmarkingBest Practice AnalysisBrainBrain Nervous SystemBrain Research through Advancing Innovative Neurotechnologies initiativeCalibrationCell SizeCodeCoding SystemCognitionDevelopmentDiseaseDisorderElectrophysiologyElectrophysiology (science)EncephalonEngineeringEsthesiaFunctional ImagingHealthHeatingHolographyIlluminationImageLaser ElectromagneticLaser RadiationLasersLightLightingMeasuresMediatingMembraneMicroscopeMicroscopyMonitorMorphologic artifactsMotionMsecNerve CellsNerve UnitNeural CellNeurocyteNeuronsNeurophysiology / ElectrophysiologyNeurosciences ResearchOpsinOpticsPerformancePhotoradiationPhysiologic ImagingPopulationProcessResolutionRod-OpsinSamplingScanningSensationShapesSourceSpeedSpottingsSystemTechnologyTestingTimeTwo HybridUpdateWritingYeast One Hybrid SystemYeast One/Two-Hybrid Systembenchmarkcomputer generateddevelopmentalelectrophysiologicalimagingimaging approachimaging based approachimaging platformin vivolight scatteringmembrane structuremicrobialmicroscope imagingmicroscopic imagingmicroscopy imagingmillisecondneuralneural controlneural imagingneural networkneural patterningneural regulationneuro-imagingneuroimagingneurological imagingneuromodulationneuromodulatoryneuronalneuroregulationnew approachesnew technologynovelnovel approachesnovel strategiesnovel strategynovel technologiesopticaloptogeneticsphysiological imagingredshiftresolutionsscale upsensorspatiotemporaltemporal measurementtemporal resolutionthree dimensionaltime measurementtwo-photonvoltageyeast two hybrid system
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Full Description

PROJECT SUMMARY
Achieving a detailed understanding of the neural codes of sensation, action, and cognition will require technologies that can both sample and perturb neural activity with millisecond precision and cellular resolution across large populations of neurons. We will develop an all-optical holographic two-photon microscope that can simultaneously record and perturb population neural activity with cellular resolution and millisecond precision. To achieve this, we will leverage multispectral temporally focused three-dimensional (3D) wavefront shaping. This new form of hybrid two-photon functional imaging will enable simultaneous illumination of user-defined ensembles of neurons in 3D with cell-size spots of two-photon excitation light at two different wavelengths – one for imaging a voltage sensor and one for controlling neural activity optogenetically. The two holographic optical paths will be completely independent and update at >kilohertz speed with the ability to sample and perturb the membrane voltage of tens to hundreds of neurons at a time. In tandem, we will develop task-optimized two-photon excitable red-shifted genetically encoded voltage sensors (GEVIs) and ultrapotent blue-shifted microbial opsins that are spectrally separable. The development of an all-holographic read/write microscope will permit neuronal recording and perturbation on spatial and temporal scales that are currently well beyond reach, which could substantially facilitate systems neuroscience research.

Grant Number: 1RF1NS131075-01
NIH Institute/Center: NIH

Principal Investigator: Hillel Adesnik

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